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Medical Device Technical Writer Jobs (NOW HIRING)

As a Technical Reviewer, you will work with medical device manufacturers throughout their ... writing skills, client and project management. You will assess cutting edge technology that will ...

As a Technical Reviewer, you will work with medical device manufacturers throughout their ... writing skills, client and project management. You will assess cutting edge technology that will ...

As a Technical Reviewer, you will work with medical device manufacturers throughout their ... writing skills, client and project management. You will assess cutting edge technology that will ...

As a Technical Reviewer, you will work with medical device manufacturers throughout their ... writing skills, client and project management. You will assess cutting edge technology that will ...

As a Technical Reviewer, you will work with medical device manufacturers throughout their ... writing skills, client and project management. You will assess cutting edge technology that will ...

As a Technical Reviewer, you will work with medical device manufacturers throughout their ... writing skills, client and project management. You will assess cutting edge technology that will ...

Medical Device Assembly

Wixom, MI · On-site

$16 - $17/hr

Ability to read and follow work instructions, BOMs, and technical drawings * Strong attention to ... Excel Medical Products is a trusted name in the medical device manufacturing industry, proudly ...

Medical Device Assembly

Wixom, MI · On-site

$16 - $17/hr

Ability to read and follow work instructions, BOMs, and technical drawings * Strong attention to ... Excel Medical Products is a trusted name in the medical device manufacturing industry, proudly ...

Bachelor's degree in medical laboratory sciences, biology, chemistry, or another relevant ... BioPharma Technical Writer I * Minimum of two (2) years of scientific or technical writing ...

Bachelor's degree in medical laboratory sciences, biology, chemistry, or another relevant ... BioPharma Technical Writer I * Minimum of two (2) years of scientific or technical writing ...

Medical Device Assembly

Wixom, MI · On-site

$16 - $17/hr

Ability to read and follow work instructions, BOMs, and technical drawings * Strong attention to ... Excel Medical Products is a trusted name in the medical device manufacturing industry, proudly ...

Assembler - Medical Device Location: Pittsburgh, PA ZIP Code: 15238 Start Date: Right Away Keywords ... Ability to read and follow technical instructions and documentation. * Basic proficiency with ...

Showing results 41-60

Medical Device Technical Writer information

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How much do medical device technical writer jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for medical device technical writer in the United States is $38.64, according to ZipRecruiter salary data. Most workers in this role earn between $26.20 and $48.80 per hour, depending on experience, location, and employer.

What is a medical device technical writer?

A Medical Device Technical Writer creates clear, accurate documentation for medical devices, including user manuals, regulatory submissions, and technical reports. They translate complex technical information into understandable content for various audiences, such as healthcare professionals, regulatory agencies, and end-users. This role requires knowledge of medical device regulations, engineering concepts, and technical writing standards. Strong attention to detail and collaboration with engineers, regulatory specialists, and subject matter experts are essential.

What are the typical day-to-day responsibilities of a medical device technical writer?

As a Medical Device Technical Writer, your daily responsibilities usually include creating and revising user manuals, product instructions, and regulatory documentation for medical devices. You'll often collaborate closely with subject matter experts such as engineers, product managers, and quality assurance teams to gather technical details and ensure accuracy. You may also be involved in reviewing documents for compliance with industry regulations and standards, as well as participating in document audits or updates. The role requires balancing multiple projects and deadlines while ensuring all materials are clear, concise, and suitable for their intended audience.

What are the key skills and qualifications needed to thrive as a medical device technical writer?

To thrive as a Medical Device Technical Writer, you need a deep understanding of medical terminology, regulatory standards, and technical writing best practices, typically supported by a degree in science, engineering, or technical communication. Familiarity with document management systems, authoring tools (such as Adobe FrameMaker or MadCap Flare), and knowledge of FDA or ISO documentation requirements are often essential. Exceptional attention to detail, strong organizational skills, and clear communication help writers collaborate effectively with engineers, clinicians, and regulatory teams. These skills and attributes ensure that complex medical device information is accurately documented, compliant with regulations, and accessible to diverse stakeholders.

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Infographic showing various Medical Device Technical Writer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 15% Part Time, and 7% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $80,364 per year, or $38.6 per hour.

Technical Specialist - Active Medical Devices

BSI Prof Serv EHS West

On-site

Full-time

Re-posted 6 days ago


Job description

We exist to create positive change for people and the planet. Join us and make a difference too!

Job title: Technical Specialist & Scheme Manager - Active Devices

Location: Global Homebased

BSI is seeking experienced medical device professionals to join our Active Medical Devices team as a home-based Technical Specialist and Certification Scheme Manager (Final Reviewer). If you have hands-on experience in the research, design, manufacture or testing of active devices we'd love to hear from you.

As a Technical Reviewer, you will work with medical device manufacturers throughout their certification life cycle to place active medical devices on the European market. This position applies a mix of engineering and design knowledge, newfound regulatory expertise, English writing skills, client and project management. You will assess cutting edge technology that will make a difference in patient health and safety and broaden your technical knowledge through ongoing training.

Responsibilities:

  • Review and evaluate medical device technical and clinical documentation in your areas of competence to assess compliance with MDD 93/42/EEC, MDR 2017/745 and UK MDR 2012 schemes.

  • Manage certification activities for a portfolio of medical device manufacturers, including determination of auditing requirements and making recommendations for the issue and maintenance of CE certifications.

  • Provide specialist regulatory, operational and strategic support to medical device scheme managers, products specialists and the business in the delivery of CE medical device marking schemes.

  • Provide Medical Device expertise leadership and mentoring in areas of competence to medical devices personnel.

To be successful in this role, you will have:

  • Four years' professional experience in the field of healthcare products or related activities, such as in manufacturing, auditing or research, of which two years shall be in thedesign, manufacture, testing or use of the device or technology to be assessedor related to the scientific aspects to be assessed.

  • Bachelor's or higher degree in a discipline relevant to the medical device industry. This may includeelectronic/electrical,electro-mechanical or biomedical engineering or medical physics.

  • Familiarity with the Medical Devices Regulation (EU)2017/745 and/ or Medical Devices Directive 96/42/EEC is an advantage.

  • At minimum, an awareness of the requirements of IEC 60601 family of standards and the risk management standard ISO 14971.

  • Understanding of the principles of design control and risk management.

  • Strong interpersonal communication skills.

  • Ability of prioritizing and executing individual workload.

  • Candidates with professional experience gained in accredited testing laboratories and a broad exposure to a range of active medical devices have been successful in the role.

Interested? To apply for this role please submit your application today and take the next step in your career as a Technical Reviewer with BSI.

BSI offers a competitive total reward package, an independent and varied job in an international environment, flexible working hours, ongoing training and development. The salary for this position for the UK can range from 58,500- 78,000 annually; actual compensation is based on various factors, including but not limited to, the candidate's competencies, level of experience, education, location, divisional budget and internal peer compensation comparisons. If you are based in the EU, your recruiter can inform you of the local salary banding which differs per country based on various factors.

Do you believe the world deservesexcellence?

We are proud to be the business improvement company for other organisations to become more sustainable and resilient and finally to inspire trust in their products, systems, services, and the world we live in.

Headquartered in London, BSI is the world's first national standards organization with more than 100 years of experience. We are a global partner for 86,000 companies and organizations in over 193 countries, offering development, auditing, certification, and training services, including innovative software solutions and cyber security expertise for all industries: from aerospace and automotive to food, construction, energy, healthcare, IT and trade sectors. Incorporated by Royal Charter, we're truly impartial, and home to the ultimate mark of trust, the Kitemark.

Through our unique combination of consulting, training, assurance and regulatory services we bring solid and broad knowledge to every company.

If you want to contribute to this inspiring challenge, bring your open and enthusiastic mindset to our dynamic team, apply now and become part of the BSI family!

D&I Policy

BSI is committed to ensuring the diversity of our workforce reflects that of our clients and the communities in which we operate.Our goal is to create a sense of belonging for all employees by providing opportunities to develop, grow, andengage with our global organization all while having fun doing great work.BSI is a community where everyone can thrive.

If you require any reasonable accommodations to be made on account of a disability orimpairment throughout out our recruiting process,please inform your Talent Acquisition Partner.

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About Us

BSI is a business improvement and standards company and for over a century BSI has been recognized for having a positive impact on organizations and society, building trust and enhancing lives.
Today BSI partners with more than 77,500 clients in 195 countries and engages with a 15,000 strong global community of experts, industry and consumer groups, organizations and governments.
Utilizing its extensive expertise in key industry sectors - including automotive, aerospace, built environment, food and retail, and healthcare - BSI delivers on its purpose by helping its clients fulfil theirs.
Living by our core values of Client-Centricity, Agility, and Collaboration, BSI provides organizations with the confidence to grow by partnering with them to tackle society's critical issues - from climate change to building trust in digital transformation and everything in between - to accelerate progress towards a better society and a sustainable world.

BSI is an Equal Opportunity Employer dedicated to fostering a diverse and inclusive workplace.